Canonical Allele Identifier: CA2812634495

Gene: ATP8B1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.57674756_57674757insTG , CM000680.2:g.57674756_57674757insTG	GRCh38
NC_000018.9:g.55341988_55341989insTG , CM000680.1:g.55341988_55341989insTG	GRCh37
NC_000018.8:g.53492986_53492987insTG	NCBI36
NG_007148.2:g.133339_133340insCA
NG_007148.3:g.134066_134067insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000642462.1:c.1819+77_1819+78insCA	ENSP00000494712.1:n.1819+77_1819+78insCA
ENST00000648039.1:c.1819+77_1819+78insCA	ENSP00000497863.1:n.1819+77_1819+78insCA
ENST00000648467.1:c.1684+77_1684+78insCA
ENST00000648908.2:c.1819+77_1819+78insCA MANE Select	ENSP00000497896.1:n.1819+77_1819+78insCA
ENST00000283684.8:c.1819+77_1819+78insCA	ENSP00000283684.4:n.1819+77_1819+78insCA
ENST00000536015.5:c.1819+77_1819+78insCA	ENSP00000445359.1:n.1819+77_1819+78insCA
NM_005603.4:c.1819+77_1819+78insCA	NP_005594.1:n.1819+77_1819+78insCA
XM_006722481.2:c.1819+77_1819+78insCA	XP_006722544.1:n.1819+77_1819+78insCA
XM_011526020.1:c.1819+77_1819+78insCA	XP_011524322.1:n.1819+77_1819+78insCA
XM_011526021.1:c.1819+77_1819+78insCA	XP_011524323.1:n.1819+77_1819+78insCA
XM_011526022.1:c.1819+77_1819+78insCA	XP_011524324.1:n.1819+77_1819+78insCA
XM_011526023.1:c.1705+77_1705+78insCA	XP_011524325.1:n.1705+77_1705+78insCA
XM_011526024.1:c.1099+77_1099+78insCA	XP_011524326.1:n.1099+77_1099+78insCA
NM_005603.6:c.1819+77_1819+78insCA	NP_005594.2:n.1819+77_1819+78insCA
XM_006722481.4:c.1819+77_1819+78insCA	XP_006722544.1:n.1819+77_1819+78insCA
XM_011526023.3:c.1705+77_1705+78insCA	XP_011524325.1:n.1705+77_1705+78insCA
NM_001374385.1:c.1819+77_1819+78insCA MANE Select	NP_001361314.1:n.1819+77_1819+78insCA
NM_001374386.1:c.1669+77_1669+78insCA	NP_001361315.1:n.1669+77_1669+78insCA